A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703200



Internal ID15093166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128103561..128103682hg38UCSC Ensembl
Innerchr10:129901825..129901946hg19UCSC Ensembl
Innerchr10:129791815..129791936hg18UCSC Ensembl
Innerchr10:129791815..129791936hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38122
hg19122
hg18122
hg17122
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516114
Supporting Variants
Samples
Known GenesMKI67
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703200
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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